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Mipomersen, an apolipoprotein B synthesis inhibitor, for lowering of LDL cholesterol concentrations in patients with homozygous familial hypercholesterolaemia: a randomised, double-blind, placebo-controlled trial.
Author: BlomDirk J, CharngMin-Ji, Chasan-TaberScott, CromwellWilliam C, CrookeStanley T, FlaimJoann D, GaudetDaniel, LachmannRobin H, MaraisA David, RaalFrederick J, SantosRaul D, TanJu L, TribbleDiane L
Original Abstract of the Article :
Homozygous familial hypercholesterolaemia is a rare genetic disorder in which both LDL-receptor alleles are defective, resulting in very high concentrations of LDL cholesterol in plasma and premature coronary artery disease. This study investigated whether an antisense inhibitor of apolipoprotein B ...See full text at original site
Dr.Camel's Paper Summary Blogラクダ博士について
ラクダ博士は、Health Journal が論文の内容を分かりやすく解説するために作成した架空のキャラクターです。
難解な医学論文を、専門知識のない方にも理解しやすいように、噛み砕いて説明することを目指しています。
* ラクダ博士による解説は、あくまで論文の要点をまとめたものであり、原論文の完全な代替となるものではありません。詳細な内容については、必ず原論文をご参照ください。
* ラクダ博士は架空のキャラクターであり、実際の医学研究者や医療従事者とは一切関係がありません。
* 解説の内容は Health Journal が独自に解釈・作成したものであり、原論文の著者または出版社の見解を反映するものではありません。
引用元:
https://doi.org/10.1016/S0140-6736(10)60284-X
データ提供:米国国立医学図書館(NLM)
Mipomersen: A New Hope for Homozygous Familial Hypercholesterolaemia
The realm of [lipid metabolism] presents unique challenges when addressing [homozygous familial hypercholesterolaemia], a rare genetic disorder characterized by extremely high levels of [LDL cholesterol]. This study investigates the efficacy and safety of [mipomersen], an [antisense inhibitor of apolipoprotein B synthesis], as an adjunctive therapy to lower [LDL cholesterol] in patients with this debilitating condition. The authors demonstrate the potential of [mipomersen] to significantly reduce [LDL cholesterol] levels, offering a glimmer of hope for patients facing the devastating consequences of this disease.
A Ray of Light in the Desert of Hypercholesterolaemia
The authors shed light on the potential of [mipomersen] to offer significant benefits for patients with [homozygous familial hypercholesterolaemia]. This research provides a glimmer of hope in the desert of this rare and challenging condition, offering a promising new treatment option for those affected by this debilitating disease.
Navigating the Desert of Lipid Management: A New Tool for Clinicians
This research equips clinicians with a valuable new tool to combat the challenges of [homozygous familial hypercholesterolaemia]. The authors provide evidence-based information to guide treatment decisions, demonstrating the efficacy and safety of [mipomersen] in lowering [LDL cholesterol] levels. This research provides an oasis of knowledge in the vast desert of lipid management.
Dr.Camel's Conclusion
This study is a reminder that even in the most desolate areas of medical knowledge, we can find hope and innovation. The development of [mipomersen] represents a significant step forward in the treatment of [homozygous familial hypercholesterolaemia], offering a glimmer of hope for patients facing a challenging journey. Let us embrace this research as a reminder to never cease exploring the vast desert of medical knowledge, seeking new solutions to improve patient outcomes.
Date :
- Date Completed 2010-05-03
- Date Revised 2015-06-16
Further Info :
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